Canonical Allele Identifier: CA2333970924
Gene: WDR62 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.36102068C= , CM000681.2:g.36102068C= GRCh38
NC_000019.9:g.36592970C= , CM000681.1:g.36592970C= GRCh37
NC_000019.8:g.41284810C= NCBI36
NG_028101.1:g.52188C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000270301.12:c.3137C= ENSP00000270301.6:p.Pro1046=
ENST00000401500.7:c.3137C= MANE Select ENSP00000384792.1:p.Pro1046=
ENST00000587391.6:c.*2412C= ENSP00000465525.1:n.*2412C=
ENST00000679357.1:c.927C=
ENST00000679422.1:c.816C=
ENST00000679682.1:c.3122C= ENSP00000506226.1:p.Pro1041=
ENST00000679714.1:c.3131C= ENSP00000506627.1:p.Pro1044=
ENST00000679757.1:c.2786C= ENSP00000505158.1:p.Pro929=
ENST00000679858.1:c.*2519C= ENSP00000505655.1:n.*2519C=
ENST00000680211.1:c.-263C= ENSP00000506102.1:n.-263C=
ENST00000680349.1:n.1120C=
ENST00000680403.1:c.3137C= ENSP00000505677.1:p.Pro1046=
ENST00000680564.1:c.2972-669C= ENSP00000505582.1:n.2972-669C=
ENST00000680590.1:c.*1532C= ENSP00000505350.1:n.*1532C=
ENST00000680739.1:c.55C=
ENST00000680773.1:n.1053C=
ENST00000680806.1:c.*1855C= ENSP00000506418.1:n.*1855C=
ENST00000680997.1:n.484C=
ENST00000681088.1:c.799C=
ENST00000681608.1:n.85C=
ENST00000681625.1:c.*469C= ENSP00000505555.1:n.*469C=
ENST00000270301.11:c.3137C= ENSP00000270301.6:p.Pro1046=
ENST00000401500.6:c.3137C= ENSP00000384792.1:p.Pro1046=
ENST00000587391.5:c.*2412C= ENSP00000465525.1:n.*2412C=
NM_001083961.1:c.3137C= NP_001077430.1:p.Pro1046=
NM_173636.4:c.3137C= NP_775907.4:p.Pro1046=
XM_005258809.2:c.3026C= XP_005258866.1:p.Pro1009=
XM_011526837.1:c.3122C= XP_011525139.1:p.Pro1041=
XM_011526838.1:c.2972-669C= XP_011525140.1:n.2972-669C=
XM_011526839.1:c.2786C= XP_011525141.1:p.Pro929=
XM_011526840.1:c.2129C= XP_011525142.1:p.Pro710=
XM_011526841.1:c.1715C= XP_011525143.1:p.Pro572=
XM_011526842.1:c.1568C= XP_011525144.1:p.Pro523=
XM_011526843.1:c.884C= XP_011525145.1:p.Pro295=
XM_011526844.1:c.884C= XP_011525146.1:p.Pro295=
XM_011526840.2:c.2129C= XP_011525142.1:p.Pro710=
XM_011526841.2:c.1715C= XP_011525143.1:p.Pro572=
XM_011526844.2:c.884C= XP_011525146.1:p.Pro295=
XM_017026665.1:c.3137C= XP_016882154.1:p.Pro1046=
NM_001083961.2:c.3137C= MANE Select NP_001077430.1:p.Pro1046=
NM_173636.5:c.3137C= NP_775907.4:p.Pro1046=